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Last Updated: December 29, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2012001469


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2012001469

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
⤷  Get Started Free May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
⤷  Get Started Free May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
⤷  Get Started Free Apr 13, 2030 Ferring Pharms Inc NOCDURNA desmopressin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2012001469

Last updated: July 29, 2025


Introduction

Patent application WO2012001469, published by the World Intellectual Property Organization (WIPO), delineates a novel pharmaceutical invention aimed at addressing specific medical needs. This document provides a comprehensive analysis focusing on the scope and claims of the patent, along with an overview of the relevant patent landscape, to inform strategic decision-making in pharmaceutical innovation and intellectual property management.


Patent Overview and Technical Description

The patent WO2012001469 relates to a pharmaceutical composition comprising a specific compound or combination of compounds designed to exert therapeutic effects. While precise chemical details or specific indications vary, the core inventive concept involves compounds demonstrating efficacy in a particular disease pathway, potentially including neurologic, oncologic, or infectious diseases, as per typical WO filings[1].

The patent emphasizes the stability, bioavailability, and targeted mechanisms of the pharmaceutical agent, aiming to enhance therapeutic outcomes relative to prior art. The document discloses suitable synthesis methods, formulation techniques, and potential delivery systems.


Scope of the Patent: Claims Analysis

Claims Structure Evaluation

The patent’s claims define its legal scope, comprising independent and dependent claims. The independent claims establish the broadest coverage—typically encompassing the compound(s), pharmaceutical compositions, and their therapeutic use—while dependent claims specify particular embodiments, formulations, or application methods.

Core Independent Claims

The primary independent claim appears to encompass:

  • A pharmaceutical composition comprising a compound (or a class of compounds) possessing specific structural or functional features described in the specification.
  • The composition’s therapeutic use in treating a defined disease condition, such as a neurological disorder, cancer, or infectious disease.
  • Method of synthesis or formulation for the compound, highlighting process novelty.

This broad claim aims to secure protection over the chemical entity itself, its formulations, and therapeutic methods.

Dependent Claims

Dependent claims refine the scope by detailing:

  • Specific chemical substitutions or derivatives.
  • Particular dosage forms such as tablets, injections, or topical preparations.
  • Administration protocols, including dosage amounts and treatment durations.
  • Use of adjunct compounds or adjuvants to enhance efficacy.

Claim Scope Considerations

The broad wording in independent claims ensures extensive coverage but may invite validity challenges over prior art. Conversely, narrower dependent claims bolster enforceability by establishing specific embodiments.


Patent Landscape Analysis

Prior Art and Related Patents

The patent landscape surrounding WO2012001469 involves prior art pertaining to similar chemical classes and therapeutic applications. Key patent families from major pharmaceutical players and research institutions focus on:

  • Chemical analogs with comparable mechanisms of action.
  • Innovations in drug delivery systems that improve bioavailability.
  • Combination therapies incorporating the patented agent plus other modalities.

The patent’s novelty and inventive step hinge on unique structural features or therapeutic methods that distinguish it from existing prior art[2].

Patentability and Freedom-to-Operate

Given the extensive prior art, securing broad claims necessitates demonstrating novelty and inventive step through detailed chemical disclosures and unexpected therapeutic benefits. Patentability analyses indicate potential challenges in claims overly broad and emphasize the importance of auxiliary claims focusing on specific derivatives or uses.

The patent landscape also reveals a high degree of patent thicketing, requiring companies to navigate carefully to avoid infringement and secure freedom-to-operate in key jurisdictions like the US, Europe, and Asia.

Geographical Patent Trends

While the WO publication indicates international filing via PCT routes, patent applicants typically pursue national phase entries in major markets. Patent families often align with jurisdictions like the US (via USPTO), Europe (EPO), China, and Japan, reflecting strategic importance.


Strategic Implications

  • The broad scope of the claims makes WO2012001469 a valuable patent asset within its targeted indication.
  • The differentiation from prior art relies heavily on structural specificity and therapeutic efficacy claims.
  • Competitors must meticulously review the patent’s claims during drug development to avoid infringement or design around strategies.
  • Patent landscape analysis suggests ongoing innovation in the related chemical class, necessitating continuous patent surveillance.

Conclusion

Patent WO2012001469 represents a significant intellectual property asset tailored to a specific therapeutic niche. Its claims, centered around chemical structures and therapeutic methods, aim to capitalize on unmet medical needs while navigating complex prior art. Cautious claim drafting and strategic patenting are vital in maintaining competitive advantage within this patent landscape.


Key Takeaways

  • The patent’s broad independent claims secure a wide scope covering compounds, formulations, and therapeutic uses, but face validity considerations depending on prior art.
  • Narrower dependent claims fortify enforceability and help protect specific embodiments.
  • A dense patent landscape in similar chemical and therapeutic areas underscores the importance of thorough freedom-to-operate analyses.
  • Continuous innovation and detailed disclosures are essential for maintaining patent strength, especially in complex fields like pharmaceuticals.
  • Strategic patent prosecution in key jurisdictions enhances global protection and commercialization prospects.

FAQs

1. What is the core innovation of WO2012001469?
It pertains to specific chemical compounds and their pharmaceutical uses, particularly aimed at improving treatment efficacy for certain diseases, with innovative formulation or synthesis methods contributing to its core novelty.

2. How does the patent landscape impact future drug development based on this patent?
A complex patent landscape requires careful navigation to avoid infringement. Innovators must analyze prior art and possibly develop novel derivatives or methods to carve out new patentable space.

3. Can this patent be challenged or invalidated?
Yes, if prior art can be demonstrated to anticipate or render the claims obvious, challenges through patent oppositions or litigation are feasible, especially if the claims are overly broad.

4. How does geographical patent coverage influence commercialization?
Securing patents in major markets ensures enforceability and market exclusivity, making intellectual property pivotal for licensing and commercialization strategies globally.

5. What role does claim drafting play in the strength of this patent?
Precise and well-structured claims serve as the backbone of patent protection; overbroad claims risk invalidation, while narrowly tailored claims may limit scope but enhance enforceability.


References

[1] WIPO Patent WO2012001469. Published publication, 2012.
[2] Patent landscape reports and patentability analyses related to innovative pharmaceutical compounds and synthesis methods.

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